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Zenger
Zenger
Health
Ben Barry

Young Newborn Survives And Thrives After Heart Surgery That Was Wired The Wrong Way

Evelina Childrens Hospital, London, United Kingdom, Architect Hopkins Architects, 2005, Evelina Childrens Hospital Exterior General View. Young Daphne Payne was born and had her surgery at Evelina Childrens Hospital. UNIVERSAL IMAGES GROUP/SWNS TALKER

A miracle baby born with her heart ‘wired’ the wrong way around survived major surgery at just eight days old and is now home and hitting all her milestones.

Daphne Payne recovering from surgery. Now at five-months-old, young Daphne had a congenital heart defect that required surgery. HAYLEY FARRER/SWNS TALKER

Daphne Payne, now five-months-old, was born with a congenital heart defect known as transposition of the great arteries – where the two main blood vessels leaving the heart are swapped over.

Her mom, Hayley Farrer, 35, was told at her 20-week scan that there was something wrong with Daphne’s heart and was given the diagnosis a few days later.

Hayley and her partner started to frantically Google to find out more about the condition.

Mom Hayley Farrer, dad Kris Payne and Daphne Payne. Family photo after the surgery, which young Daphne is in high spirits. HAYLEY FARRER/SWNS TALKER

Doctors originally planned to induce Hayley, so she could give birth by C-section, but Daphne’s heartbeat kept dropping.

After being closely monitored by hospital staff, Daphne was delivered naturally on August 26, 2022, at 38 weeks, weighing 6lb 13oz and is now hitting “every milestone.”

Hayley Farrer, 35, a police officer from Fleet, UK, said: “You would never think she would have been through what she had been through.

“She is growing really well. She is six months on Sunday, and she is developing really well.

“She is like any other baby – made of tough stuff.”

Daphne Payne in the hospital. Daphne underwent her first operation at just two-days-old to keep a small gap open in her heart, called an atrial septostomy. HAYLEY FARRER/SWNS TALKER

After being diagnosed with a heart defect Daphne was born at the Evelina London Children’s Hospital, London.

Daphne was taken to the neonatal intensive care unit, with mom Hayley seeing her for the first time nine hours after her birth.

Daphne underwent her first operation at just two-days-old to keep a small gap open in her heart, called an atrial septostomy – a procedure where a small hole is made in the wall between the left and right atria of the heart.

Eight days later, she had an arterial switch – open-heart surgery to move the two major blood vessels into the correct place.

Daphne Payne pictured on the couch. Daphne spent two weeks in the specialist children’s hospital before being able to come home in September 2022 just 16 days old. HAYLEY FARRER/SWNS TALKER

The operation involves cutting off the aorta and pulmonary arteries just above the point where they leave the heart.

Hayley said: “The doctors told me there was a 98 percent success rate with the surgery.

“When she went down I was really positive, but there is always something in the back of your mind saying that someone has to be the two percent.”

Daphne spent two weeks in the specialist children’s hospital before being able to come home in September 2022 just 16 days old.

The mom-of-one said: “I’m so grateful for all the care Daphne and I received from the maternity team at St Thomas’ and the cardiology teams at Evelina London Children’s Hospital.

“She has hit every milestone. She is so strong.”

Daphne’s uncle, Paul Farrer, 40, a firefighter, will be running the London Marathon to thank the cardiology team at Evelina London Children’s Hospital for saving her life.

Paul, from Walton-on-Thames, said: “My sister Hayley found out at her 20-week scan that Daphne had a rare, congenital heart defect.

“We knew that Daphne would need specialist heart surgery soon after birth, so Hayley had her antenatal care moved to St Thomas’ Hospital.

“She had this amazing, positive outlook even after Daphne’s diagnosis.”

Paul is taking on the TSC London Marathon on April 23 to raise funds for Evelina London Children’s Charity.

Produced in association with SWNS Talker

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